Assisted reproduction embryo-assessment software - UK MHRA Medical Device Registration

Assisted reproduction embryo-assessment software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178737. The device is manufactured by Life Whisperer Diagnostics Pty Ltd from Australia, classified as General Medical Device. The authorized representative in the UK is QAdvis UK Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Assisted reproduction embryo-assessment software

MHRA Device ID: 178737•Ref: 178737

Device Type

General Medical Device

Devices

Assisted reproduction embryo-assessment software

Type

Class I

Date Registered

Oct 4, 2024

Last Updated

Nov 7, 2023

Manufacturer Information

Name

Life Whisperer Diagnostics Pty Ltd

Address

Company No: 616270798 Level 2, Tech_Central Lot Fourteen Frome Road

Adelaide, Australia

Created Date

Dec 21, 2021

Authorized Representative

Name

QAdvis UK Ltd

Relationship Type

UK Responsible Person

Address

55-66 Frederick Street

Edinburgh, EH2 1LS, Scotland, United Kingdom

Postcode: EH2 1LS

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Other Products from Life Whisperer Diagnostics Pty Ltd (1)

Assisted reproduction embryo-assessment software

Type: General Medical Device

Registered: Oct 4, 2024

Other Products from Same Authorized Representative (10)

Assisted reproduction embryo-assessment software - UK MHRA Medical Device Registration

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